Literature DB >> 15568946

Optimizing low-light microscopy with back-illuminated electron multiplying charge-coupled device: enhanced sensitivity, speed, and resolution.

Colin G Coates1, Donal J Denvir, Noel G McHale, Keith D Thornbury, Mark A Hollywood.   

Abstract

The back-illuminated electron multiplying charge-coupled device (EMCCD) camera is having a profound influence on the field of low-light dynamic cellular microscopy, combining highest possible photon collection efficiency with the ability to virtually eliminate the readout noise detection limit. We report here the use of this camera, in 512 x 512 frame-transfer chip format at 10-MHz pixel readout speed, in optimizing a demanding ultra-low-light intracellular calcium flux microscopy setup. The arrangement employed includes a spinning confocal Nipkow disk, which, while facilitating the need to both generate images at very rapid frame rates and minimize background photons, yields very weak signals. The challenge for the camera lies not just in detecting as many of these scarce photons as possible, but also in operating at a frame rate that meets the temporal resolution requirements of many low-light microscopy approaches, a particular demand of smooth muscle calcium flux microscopy. Results presented illustrate both the significant sensitivity improvement offered by this technology over the previous standard in ultra-low-light CCD detection, the GenIII+intensified charge-coupled device (ICCD), and also portray the advanced temporal and spatial resolution capabilities of the EMCCD. Copyright 2004 Society of Photo-Optical Instrumentation Engineers.

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Year:  2004        PMID: 15568946     DOI: 10.1117/1.1805559

Source DB:  PubMed          Journal:  J Biomed Opt        ISSN: 1083-3668            Impact factor:   3.170


  8 in total

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2.  The role of Ca(2+) influx in spontaneous Ca(2+) wave propagation in interstitial cells of Cajal from the rabbit urethra.

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3.  Nanotopology of cell adhesion upon Variable-Angle Total Internal Reflection Fluorescence Microscopy (VA-TIRFM).

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Review 4.  Optical imaging of voltage and calcium in cardiac cells & tissues.

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6.  Light dose is a limiting factor to maintain cell viability in fluorescence microscopy and single molecule detection.

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7.  Subcellular resolution three-dimensional light-field imaging with genetically encoded voltage indicators.

Authors:  Peter Quicke; Carmel L Howe; Pingfan Song; Herman V Jadan; Chenchen Song; Thomas Knöpfel; Mark Neil; Pier L Dragotti; Simon R Schultz; Amanda J Foust
Journal:  Neurophotonics       Date:  2020-08-28       Impact factor: 3.593

8.  Cholesterol dependent uptake and interaction of doxorubicin in mcf-7 breast cancer cells.

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Journal:  Int J Mol Sci       Date:  2013-04-16       Impact factor: 5.923

  8 in total

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